Authors: Yeowell, HN Walker, LC

Citation: Hn. Yeowell et Lc. Walker, Mutations in the lysyl hydroxylase 1 gene that result in enzyme deficiencyand the clinical phenotype of Ehlers-Danlos syndrome type VI, MOL GEN MET, 71(1-2), 2000, pp. 212-224

Authors: Yeowell, HN Allen, JD Walker, LC Overstreet, MA Murad, S Thai, SF

Citation: Hn. Yeowell et al., Deletion of cysteine 369 in lysyl hydroxylase 1 eliminates enzyme activityand causes Ehlers-Danlos syndrome type VI, MATRIX BIOL, 19(1), 2000, pp. 37-46

Authors: Walker, LC Marini, JC Grange, DK Filie, J Yeowell, HN

Citation: Lc. Walker et al., A patient with Ehlers-Danlos syndrome type VI is homozygous for a premature termination codon in exon 14 of the lysyl hydroxylase 1 gene, MOL GEN MET, 67(1), 1999, pp. 74-82

Authors: Yeowell, HN Walker, LC

Citation: Hn. Yeowell et Lc. Walker, Prenatal exclusion of Ehlers-Danlos Syndrome type VI by mutational analysis, P ASS AM PH, 111(1), 1999, pp. 57-62

Authors: Yeowell, HN Walker, LC

Citation: Hn. Yeowell et Lc. Walker, Tissue specificity of a new splice form of the human lysyl hydroxylase 2 gene, MATRIX BIOL, 18(2), 1999, pp. 179-187